5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

Base Information

Chemical Name:5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide
CAS No.:1612898-16-4
Molecular Formula:C₂₆H₂₆ClN₃O₃S
Molecular Weight:496.03
Hs Code.:

Synonyms:5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

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Chemical Property of 5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

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Technology Process of 5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

There total 5 articles about 5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 77.0%

: 1612898-23-3
(4-dimethylaminophenyl)methanamine trifluoroacetate

: 473257-46-4
5-chloro-3-(3,5-dimethylphenyl-sulfonyl)indole-2-carboxylic acid

: 1612898-16-4
5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

Guidance literature:: With (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In N,N-dimethyl-formamide; at 25 ℃; for 12h;
DOI:10.1016/j.ejmech.2014.04.027

Reference yield:

: 18600-42-5
4-nitrobenzylamine hydrochloride

: 1612898-16-4
5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / dichloromethane / 2 h / 0 - 20 °C

2: palladium 10% on activated carbon; hydrogen / methanol / 2 h / 20 °C / 1810.07 Torr

3: potassium carbonate / acetone / 16 h / 20 °C

4: dichloromethane / 0.5 h / 20 °C

5: triethylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 12 h / 25 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2014.04.027

Reference yield:

: 94838-58-1
tert-butyl 4-nitrobenzylcarbamate

: 1612898-16-4
5-chloro-N-(4-dimethylaminobenzyl)-3-((3,5-dimethylphenyl)sulfonyl)-1H-indole-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: palladium 10% on activated carbon; hydrogen / methanol / 2 h / 20 °C / 1810.07 Torr

2: potassium carbonate / acetone / 16 h / 20 °C

3: dichloromethane / 0.5 h / 20 °C

4: triethylamine; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate / N,N-dimethyl-formamide / 12 h / 25 °C

With palladium 10% on activated carbon; hydrogen; potassium carbonate; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; triethylamine; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1016/j.ejmech.2014.04.027